510(k) K980952 ยท LRK Device, Anti-Snoring
SNORE-CURE ANTI-SNORING APPLIANCE
| Applicant | ORTHO-TAIN, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jun 1, 1998 |
| Received | Mar 13, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980952
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.